Senior Quality Engineer - Medical Device - Canton, MA

• Support the effectiveness, maintenance, and continuous improvement of the Quality Management System (QMS).
• Partner with leadership and cross-functional teams to ensure compliance with ISO 13485 requirements.
• Mentor and train Quality Engineers while supporting onboarding and professional development initiatives.
• Provide shop floor quality support, troubleshoot manufacturing issues, and lead root cause investigations.
• Own Risk Management activities, including FMEA development and ongoing risk mitigation efforts.
• Manage customer complaints, returns, and corrective action activities to ensure timely resolution.
• Support equipment qualification and validation activities including IQ, OQ, and PQ protocols.
• Execute Measurement System Analysis (MSA) and Gage R&R studies to improve inspection reliability.
• Identify, implement, and validate new inspection technologies and quality control methods.
• Lead quality improvement projects through statistical analysis and data-driven decision-making.
• Manage engineering change processes and associated risk assessments.
• Support supplier quality activities, including Approved Supplier List evaluations and performance reviews.
• Develop and maintain quality documentation, SOPs, work instructions, and forms.
• Perform product inspections and other quality-related activities as require

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.